Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packaged in a plastic bottle with white cap.
Summary
The FDA issued a Class II for Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packa by NuNaturals Inc. Reason: Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit Sweetener..
Details
Source
Food Recall
External ID
H-0381-2025
Action Date
2025-08-06
Status
Terminated
Category
food
Product Description
Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packaged in a plastic bottle with white cap. Ingredient: Monk Fruit (Luo Han Guo) Extract. Monk Fruit is so much sweeter than sugar, a pinch is all you need. Suggested Use: Add to sweeten your food or beverage. 1/64 tsp (a pinch) tastes as sweet as 1 tsp of sugar. Distributed by: NuNaturals, Inc. Eugene, OR 97402.
Lot/Code Info: Best By 4/28 25104S Code Explained: Best By: April 2028. Lot Number: 25104S Represents date of production: YYDDD[S] YY 25 = 2025 Julian day = 104 [S] = 1 digit alpha suffix
Quantity Affected: 78 bottles (total)
Reason for Recall
Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit Sweetener.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-14
Company
Eugene, OR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
NuNaturals Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (NuNaturals Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does NuNaturals Inc have FDA actions?
NuNaturals Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0381-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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